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Implementation of PrEP Care Among Women in Family Planning Clinics

Implementation of PrEP Care Among Women in Family Planning Clinics

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06335121
Enrollment
250
Registered
2024-03-28
Start date
2026-12-01
Completion date
2027-06-01
Last updated
2026-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV, PrEP Uptake, Prevention

Brief summary

This study will evaluate implementation strategies to address barriers and increase uptake of PrEP among Black cisgender women in Planned Parenthood of Illinois (PPIL) health centers.

Interventions

BEHAVIORALPOWER Up strategies -

Clinics will implement adapted POWER Up intervention strategies when a patient is flagged as PrEP eligible.

Sponsors

Rush University Medical Center
Lead SponsorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH
University of Illinois at Chicago
CollaboratorOTHER
Planned Parenthood of Illinois
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Eligible participants include ciswomen presenting at a PPIL health center with a positive STI test (syphilis, gonorrhea, or chlamydia) and identified in the EHR using STI testing records and new fields for optimizing support of provider PrEP counseling.

Exclusion criteria

\- Participants will be excluded if they are not PrEP eligible, have a negative STI test, or are not identified in the EHR.

Design outcomes

Primary

MeasureTime frameDescription
PrEP prescriptions among Black women accessing PPIL services and eligible for PrEP.1 monthPrEP eligibility among Black women will be defined based on positive STI test and identified in the EHR using STI testing records and new fields for optimizing support of provider PrEP counseling. Using de-identified patient-level EHR data for eligible women at each clinic within each time point, we will create a dichotomous variable for having received a prescription for PrEP during a given time period.

Secondary

MeasureTime frameDescription
Receipt of PrEP refills among Black women accessing FP services at 6 months.6 monthsUsing de-identified patient-level EHR data for eligible patients at each clinic within each time point, we will create a dichotomous variable for receiving refills of prescriptions for PrEP of those with an initial PrEP prescription.

Contacts

CONTACTCristina MA Barkowski, MSW
cristina_m_barkowski@rush.edu312-942-6382
CONTACTKate P Palmer, MPH
kate_p_palmer@rush.edu312-563-9389
PRINCIPAL_INVESTIGATORSadia Haider, MD, MPH

Rush University Medical Center

PRINCIPAL_INVESTIGATORAmy Johnson, PhD, MSW

Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026